# FDA Inspection 709225 - Pulpdent Corporation - February 08, 2011

Source: https://www.keypedia.com/records/fda_inspections/pulpdent-corporation/41d9355d-e589-4532-a9df-55eed33483e4
Source feed: FDA_Inspections

> FDA Inspection 709225 for Pulpdent Corporation on February 08, 2011. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 709225
- Company Name: Pulpdent Corporation
- Inspection Date: 2011-02-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 836092 - 2013-06-11](https://www.keypedia.com/records/fda_inspections/pulpdent-corporation/7033c8bd-7cd3-464d-b4d9-c2138a64a558)
- [FDA Inspection 577342 - 2009-04-17](https://www.keypedia.com/records/fda_inspections/pulpdent-corporation/8bca3ed2-836e-4aa5-8fa2-0ac7da4db3cf)

Company: https://www.keypedia.com/companies/pulpdent-corporation/5281d2aa-860f-4197-b38e-3a80fe7f5d60

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7